A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142706



Internal ID341907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29019744..29040227hg38UCSC Ensembl
chr7:29059360..29079843hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3820484
hg1920484
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16994643
Samples
Known GenesCPVL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142706
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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